triamcinolone acetonide 32 MG Injection [Zilretta]

RxCUI: 1947133
RxNorm name: triamcinolone acetonide 32 MG Injection [Zilretta]
Display name: triamcinolone acetonide 32 MG Injection [Zilretta]
Full name: triamcinolone acetonide 32 MG Injection [Zilretta]
Term type: SBD
Status: DailyMed mapping
Updated: 2026-06-04 23:39:21

RxNav Current And Historical NDCs#

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UNII Substances#

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openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

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Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Zilretta	TRIAMCINOLONE ACETONIDE EXTENDED-RELEASE INJECTABLE SUSPENSION	Pacira Pharmaceuticals, Inc.	cd5c4673-21f2-4126-9556-da847b3a228b	2026-06-03	Warnings, Adverse reactions	Exact identifier rxcui: 1947133

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set ID	RxNorm string	TTY	SPL version	Label	Effective
cd5c4673-21f2-4126-9556-da847b3a228b	triamcinolone acetonide 32 MG Injection [Zilretta]	SBD	6	These highlights do not include all the information needed to use ZILRETTA safely and effectively. See full prescribing information for ZILRETTA. ZILRETTA ® (triamcinolone acetonide extended-release injectable suspension), for intra-articular use Initial U.S. Approval: 1957	20260402
cd5c4673-21f2-4126-9556-da847b3a228b	Zilretta 32 MG Injection	SY	6	These highlights do not include all the information needed to use ZILRETTA safely and effectively. See full prescribing information for ZILRETTA. ZILRETTA ® (triamcinolone acetonide extended-release injectable suspension), for intra-articular use Initial U.S. Approval: 1957	20260402
cd5c4673-21f2-4126-9556-da847b3a228b	Zilretta 32 MG Extended-Release Injection	PSN	6	These highlights do not include all the information needed to use ZILRETTA safely and effectively. See full prescribing information for ZILRETTA. ZILRETTA ® (triamcinolone acetonide extended-release injectable suspension), for intra-articular use Initial U.S. Approval: 1957	20260402